EP0705262A1 - Verfahren zur asymmetrischen totalsynthese von camptothecin - Google Patents
Verfahren zur asymmetrischen totalsynthese von camptothecinInfo
- Publication number
- EP0705262A1 EP0705262A1 EP94919413A EP94919413A EP0705262A1 EP 0705262 A1 EP0705262 A1 EP 0705262A1 EP 94919413 A EP94919413 A EP 94919413A EP 94919413 A EP94919413 A EP 94919413A EP 0705262 A1 EP0705262 A1 EP 0705262A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- formula
- compound
- hydrogen
- dioxolanone
- cis
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- VSJKWCGYPAHWDS-FQEVSTJZSA-N camptothecin Chemical compound C1=CC=C2C=C(CN3C4=CC5=C(C3=O)COC(=O)[C@]5(O)CC)C4=NC2=C1 VSJKWCGYPAHWDS-FQEVSTJZSA-N 0.000 title claims abstract description 42
- 238000000034 method Methods 0.000 title claims description 53
- 230000008569 process Effects 0.000 title claims description 49
- KLWPJMFMVPTNCC-UHFFFAOYSA-N Camptothecin Natural products CCC1(O)C(=O)OCC2=C1C=C3C4Nc5ccccc5C=C4CN3C2=O KLWPJMFMVPTNCC-UHFFFAOYSA-N 0.000 title claims description 13
- 229940127093 camptothecin Drugs 0.000 title claims description 13
- VSJKWCGYPAHWDS-UHFFFAOYSA-N dl-camptothecin Natural products C1=CC=C2C=C(CN3C4=CC5=C(C3=O)COC(=O)C5(O)CC)C4=NC2=C1 VSJKWCGYPAHWDS-UHFFFAOYSA-N 0.000 title claims description 13
- 238000011929 asymmetric total synthesis Methods 0.000 title description 4
- 150000001875 compounds Chemical class 0.000 claims description 60
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 claims description 48
- 229910052739 hydrogen Inorganic materials 0.000 claims description 40
- 239000001257 hydrogen Substances 0.000 claims description 40
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 36
- -1 SiMe3 Chemical group 0.000 claims description 33
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 22
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 21
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 20
- 125000000217 alkyl group Chemical group 0.000 claims description 18
- KNCYXPMJDCCGSJ-UHFFFAOYSA-N piperidine-2,6-dione Chemical compound O=C1CCCC(=O)N1 KNCYXPMJDCCGSJ-UHFFFAOYSA-N 0.000 claims description 18
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical group [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 16
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical group [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 claims description 15
- 150000001408 amides Chemical class 0.000 claims description 13
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 13
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 12
- 150000005690 diesters Chemical group 0.000 claims description 12
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims description 11
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 11
- 230000015572 biosynthetic process Effects 0.000 claims description 11
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical group I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 11
- 229910052757 nitrogen Inorganic materials 0.000 claims description 11
- WAZSVCKLDOMJJX-UHFFFAOYSA-N 2h-pyrrolo[3,4-b]quinoline Chemical compound C1=CC=CC2=CC3=CNC=C3N=C21 WAZSVCKLDOMJJX-UHFFFAOYSA-N 0.000 claims description 9
- 150000001299 aldehydes Chemical class 0.000 claims description 9
- 150000002431 hydrogen Chemical group 0.000 claims description 9
- 238000010626 work up procedure Methods 0.000 claims description 9
- WVSYONICNIDYBE-UHFFFAOYSA-N 4-fluorobenzenesulfonic acid Chemical group OS(=O)(=O)C1=CC=C(F)C=C1 WVSYONICNIDYBE-UHFFFAOYSA-N 0.000 claims description 8
- 150000004702 methyl esters Chemical group 0.000 claims description 8
- SPEUIVXLLWOEMJ-UHFFFAOYSA-N 1,1-dimethoxyethane Chemical group COC(C)OC SPEUIVXLLWOEMJ-UHFFFAOYSA-N 0.000 claims description 7
- 230000007062 hydrolysis Effects 0.000 claims description 7
- 238000006460 hydrolysis reaction Methods 0.000 claims description 7
- 239000011541 reaction mixture Substances 0.000 claims description 7
- 150000001412 amines Chemical group 0.000 claims description 6
- 150000002596 lactones Chemical class 0.000 claims description 6
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 6
- 238000006845 Michael addition reaction Methods 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 5
- 238000011914 asymmetric synthesis Methods 0.000 claims description 4
- 239000003153 chemical reaction reagent Substances 0.000 claims description 4
- 230000009467 reduction Effects 0.000 claims description 4
- 238000006798 ring closing metathesis reaction Methods 0.000 claims description 4
- 125000003158 alcohol group Chemical group 0.000 claims description 3
- 238000005882 aldol condensation reaction Methods 0.000 claims description 3
- 238000005899 aromatization reaction Methods 0.000 claims description 3
- 230000008878 coupling Effects 0.000 claims description 3
- 238000010168 coupling process Methods 0.000 claims description 3
- 238000005859 coupling reaction Methods 0.000 claims description 3
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 claims description 3
- XJDDLMJULQGRLU-UHFFFAOYSA-N 1,3-dioxane-4,6-dione Chemical class O=C1CC(=O)OCO1 XJDDLMJULQGRLU-UHFFFAOYSA-N 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims description 2
- 150000001649 bromium compounds Chemical group 0.000 claims 2
- 150000001733 carboxylic acid esters Chemical group 0.000 claims 2
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims 2
- 230000029936 alkylation Effects 0.000 claims 1
- 238000005804 alkylation reaction Methods 0.000 claims 1
- 150000001805 chlorine compounds Chemical group 0.000 claims 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 230000003301 hydrolyzing effect Effects 0.000 claims 1
- 238000010348 incorporation Methods 0.000 claims 1
- YORCIIVHUBAYBQ-UHFFFAOYSA-N propargyl bromide Chemical compound BrCC#C YORCIIVHUBAYBQ-UHFFFAOYSA-N 0.000 claims 1
- UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical group OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 claims 1
- 125000000168 pyrrolyl group Chemical group 0.000 claims 1
- 239000000543 intermediate Substances 0.000 abstract description 13
- 239000000126 substance Substances 0.000 abstract description 9
- 238000001311 chemical methods and process Methods 0.000 abstract description 2
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 56
- 239000000243 solution Substances 0.000 description 51
- 239000000047 product Substances 0.000 description 40
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 24
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 18
- 238000006243 chemical reaction Methods 0.000 description 18
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 18
- 239000000203 mixture Substances 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 15
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
- 238000003756 stirring Methods 0.000 description 13
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 12
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 11
- 239000007787 solid Substances 0.000 description 11
- KLFJSYOEEYWQMR-NRFANRHFSA-N 10-methoxycamptothecin Chemical compound C1=C(OC)C=C2C=C(CN3C4=CC5=C(C3=O)COC(=O)[C@]5(O)CC)C4=NC2=C1 KLFJSYOEEYWQMR-NRFANRHFSA-N 0.000 description 10
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 10
- 150000004820 halides Chemical class 0.000 description 10
- 239000003921 oil Substances 0.000 description 10
- 235000019198 oils Nutrition 0.000 description 10
- WJKHJLXJJJATHN-UHFFFAOYSA-N triflic anhydride Chemical compound FC(F)(F)S(=O)(=O)OS(=O)(=O)C(F)(F)F WJKHJLXJJJATHN-UHFFFAOYSA-N 0.000 description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 8
- 239000012298 atmosphere Substances 0.000 description 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 8
- 239000000741 silica gel Substances 0.000 description 8
- 229910002027 silica gel Inorganic materials 0.000 description 8
- 229960000583 acetic acid Drugs 0.000 description 7
- 238000004128 high performance liquid chromatography Methods 0.000 description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
- FJJYHTVHBVXEEQ-UHFFFAOYSA-N 2,2-dimethylpropanal Chemical compound CC(C)(C)C=O FJJYHTVHBVXEEQ-UHFFFAOYSA-N 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 239000002585 base Substances 0.000 description 6
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 6
- 239000003480 eluent Substances 0.000 description 6
- 238000001914 filtration Methods 0.000 description 6
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 6
- 239000007858 starting material Substances 0.000 description 6
- XVMZDZFTCKLZTF-UHFFFAOYSA-N 9-methoxycamtothecin Natural products C1=CC(OC)=C2C=C(CN3C4=CC5=C(C3=O)COC(=O)C5(O)CC)C4=NC2=C1 XVMZDZFTCKLZTF-UHFFFAOYSA-N 0.000 description 5
- KLFJSYOEEYWQMR-UHFFFAOYSA-N CPT-OMe Natural products C1=C(OC)C=C2C=C(CN3C4=CC5=C(C3=O)COC(=O)C5(O)CC)C4=NC2=C1 KLFJSYOEEYWQMR-UHFFFAOYSA-N 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
- 239000012230 colorless oil Substances 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- 238000001704 evaporation Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 239000012044 organic layer Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 5
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 5
- AFENDNXGAFYKQO-GSVOUGTGSA-N (R)-2-hydroxybutyric acid Chemical compound CC[C@@H](O)C(O)=O AFENDNXGAFYKQO-GSVOUGTGSA-N 0.000 description 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 4
- KZMGYPLQYOPHEL-UHFFFAOYSA-N Boron trifluoride etherate Chemical compound FB(F)F.CCOCC KZMGYPLQYOPHEL-UHFFFAOYSA-N 0.000 description 4
- 238000005481 NMR spectroscopy Methods 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 4
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 4
- 125000003262 carboxylic acid ester group Chemical group [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 description 4
- 238000004587 chromatography analysis Methods 0.000 description 4
- JHCKGVJZNIWNJK-UHFFFAOYSA-N diethyl pent-2-enedioate Chemical compound CCOC(=O)CC=CC(=O)OCC JHCKGVJZNIWNJK-UHFFFAOYSA-N 0.000 description 4
- 230000008020 evaporation Effects 0.000 description 4
- 150000002465 imidoyl halides Chemical class 0.000 description 4
- ZCSHNCUQKCANBX-UHFFFAOYSA-N lithium diisopropylamide Chemical compound [Li+].CC(C)[N-]C(C)C ZCSHNCUQKCANBX-UHFFFAOYSA-N 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- 230000004044 response Effects 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- 238000004809 thin layer chromatography Methods 0.000 description 4
- HFRXJVQOXRXOPP-UHFFFAOYSA-N thionyl bromide Chemical compound BrS(Br)=O HFRXJVQOXRXOPP-UHFFFAOYSA-N 0.000 description 4
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 4
- 238000006257 total synthesis reaction Methods 0.000 description 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- DGHHQBMTXTWTJV-BQAIUKQQSA-N 119413-54-6 Chemical compound Cl.C1=C(O)C(CN(C)C)=C2C=C(CN3C4=CC5=C(C3=O)COC(=O)[C@]5(O)CC)C4=NC2=C1 DGHHQBMTXTWTJV-BQAIUKQQSA-N 0.000 description 3
- 238000005160 1H NMR spectroscopy Methods 0.000 description 3
- HZNVUJQVZSTENZ-UHFFFAOYSA-N 2,3-dichloro-5,6-dicyano-1,4-benzoquinone Chemical compound ClC1=C(Cl)C(=O)C(C#N)=C(C#N)C1=O HZNVUJQVZSTENZ-UHFFFAOYSA-N 0.000 description 3
- QWCKQJZIFLGMSD-GSVOUGTGSA-N D-alpha-aminobutyric acid Chemical compound CC[C@@H](N)C(O)=O QWCKQJZIFLGMSD-GSVOUGTGSA-N 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 3
- 150000001241 acetals Chemical class 0.000 description 3
- 230000000118 anti-neoplastic effect Effects 0.000 description 3
- 230000000840 anti-viral effect Effects 0.000 description 3
- SIPUZPBQZHNSDW-UHFFFAOYSA-N bis(2-methylpropyl)aluminum Chemical compound CC(C)C[Al]CC(C)C SIPUZPBQZHNSDW-UHFFFAOYSA-N 0.000 description 3
- 239000012043 crude product Substances 0.000 description 3
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 3
- 239000012362 glacial acetic acid Substances 0.000 description 3
- NPZTUJOABDZTLV-UHFFFAOYSA-N hydroxybenzotriazole Substances O=C1C=CC=C2NNN=C12 NPZTUJOABDZTLV-UHFFFAOYSA-N 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- JKANAVGODYYCQF-UHFFFAOYSA-N prop-2-yn-1-amine Chemical compound NCC#C JKANAVGODYYCQF-UHFFFAOYSA-N 0.000 description 3
- 229960000303 topotecan Drugs 0.000 description 3
- 238000010792 warming Methods 0.000 description 3
- LSTRKXWIZZZYAS-UHFFFAOYSA-N 2-bromoacetyl bromide Chemical compound BrCC(Br)=O LSTRKXWIZZZYAS-UHFFFAOYSA-N 0.000 description 2
- YEDUAINPPJYDJZ-UHFFFAOYSA-N 2-hydroxybenzothiazole Chemical compound C1=CC=C2SC(O)=NC2=C1 YEDUAINPPJYDJZ-UHFFFAOYSA-N 0.000 description 2
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 2
- IAUZDBFOEWAQFE-UHFFFAOYSA-N 3-o-benzyl 1-o-methyl propanedioate Chemical compound COC(=O)CC(=O)OCC1=CC=CC=C1 IAUZDBFOEWAQFE-UHFFFAOYSA-N 0.000 description 2
- JJHVYGVVMBYCMQ-UHFFFAOYSA-N 6-hydroxy-4-methyl-1h-pyridin-2-one Chemical compound CC=1C=C(O)NC(=O)C=1 JJHVYGVVMBYCMQ-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 2
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000002168 alkylating agent Substances 0.000 description 2
- 229940100198 alkylating agent Drugs 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 125000002619 bicyclic group Chemical group 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 235000011089 carbon dioxide Nutrition 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- QQVDYSUDFZZPSU-UHFFFAOYSA-M chloromethylidene(dimethyl)azanium;chloride Chemical compound [Cl-].C[N+](C)=CCl QQVDYSUDFZZPSU-UHFFFAOYSA-M 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000008030 elimination Effects 0.000 description 2
- 238000003379 elimination reaction Methods 0.000 description 2
- 238000010828 elution Methods 0.000 description 2
- 239000000284 extract Substances 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 239000000295 fuel oil Substances 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 2
- 150000003949 imides Chemical class 0.000 description 2
- 238000002955 isolation Methods 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 238000001819 mass spectrum Methods 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 230000010534 mechanism of action Effects 0.000 description 2
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 2
- XMJHPCRAQCTCFT-UHFFFAOYSA-N methyl chloroformate Chemical compound COC(Cl)=O XMJHPCRAQCTCFT-UHFFFAOYSA-N 0.000 description 2
- 229930014626 natural product Natural products 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- BHAAPTBBJKJZER-UHFFFAOYSA-N p-anisidine Chemical compound COC1=CC=C(N)C=C1 BHAAPTBBJKJZER-UHFFFAOYSA-N 0.000 description 2
- 230000020477 pH reduction Effects 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 230000008707 rearrangement Effects 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000012047 saturated solution Substances 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- HJUGFYREWKUQJT-UHFFFAOYSA-N tetrabromomethane Chemical compound BrC(Br)(Br)Br HJUGFYREWKUQJT-UHFFFAOYSA-N 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 2
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical class OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 2
- AFENDNXGAFYKQO-VKHMYHEASA-N (S)-2-hydroxybutyric acid Chemical compound CC[C@H](O)C(O)=O AFENDNXGAFYKQO-VKHMYHEASA-N 0.000 description 1
- DYLIWHYUXAJDOJ-OWOJBTEDSA-N (e)-4-(6-aminopurin-9-yl)but-2-en-1-ol Chemical compound NC1=NC=NC2=C1N=CN2C\C=C\CO DYLIWHYUXAJDOJ-OWOJBTEDSA-N 0.000 description 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- GZTMCZAOQTVOJK-UHFFFAOYSA-N 1,3-dioxolan-4-one Chemical compound O=C1COCO1 GZTMCZAOQTVOJK-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- 238000007115 1,4-cycloaddition reaction Methods 0.000 description 1
- VFWCMGCRMGJXDK-UHFFFAOYSA-N 1-chlorobutane Chemical compound CCCCCl VFWCMGCRMGJXDK-UHFFFAOYSA-N 0.000 description 1
- JMTMSDXUXJISAY-UHFFFAOYSA-N 2H-benzotriazol-4-ol Chemical compound OC1=CC=CC2=C1N=NN2 JMTMSDXUXJISAY-UHFFFAOYSA-N 0.000 description 1
- FPQQSJJWHUJYPU-UHFFFAOYSA-N 3-(dimethylamino)propyliminomethylidene-ethylazanium;chloride Chemical compound Cl.CCN=C=NCCCN(C)C FPQQSJJWHUJYPU-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 229910015900 BF3 Inorganic materials 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical group NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- VGCXGMAHQTYDJK-UHFFFAOYSA-N Chloroacetyl chloride Chemical compound ClCC(Cl)=O VGCXGMAHQTYDJK-UHFFFAOYSA-N 0.000 description 1
- 238000007445 Chromatographic isolation Methods 0.000 description 1
- HHLFWLYXYJOTON-UHFFFAOYSA-N Glyoxylic acid Natural products OC(=O)C=O HHLFWLYXYJOTON-UHFFFAOYSA-N 0.000 description 1
- 229910004373 HOAc Inorganic materials 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 1
- 238000006000 Knoevenagel condensation reaction Methods 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 1
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 1
- 235000019502 Orange oil Nutrition 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- AKZWRTCWNXHHFR-PDIZUQLASA-N [(3S)-oxolan-3-yl] N-[(2S,3S)-4-[(5S)-5-benzyl-3-[(2R)-2-carbamoyloxy-2,3-dihydro-1H-inden-1-yl]-4-oxo-3H-pyrrol-5-yl]-3-hydroxy-1-phenylbutan-2-yl]carbamate Chemical compound NC(=O)O[C@@H]1Cc2ccccc2C1C1C=N[C@](C[C@H](O)[C@H](Cc2ccccc2)NC(=O)O[C@H]2CCOC2)(Cc2ccccc2)C1=O AKZWRTCWNXHHFR-PDIZUQLASA-N 0.000 description 1
- 150000001347 alkyl bromides Chemical class 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 229940124277 aminobutyric acid Drugs 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 230000001093 anti-cancer Effects 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- ITRPPWFSLFFEJJ-UHFFFAOYSA-N azane dihydrobromide Chemical compound [H+].[NH4+].[Br-].[Br-] ITRPPWFSLFFEJJ-UHFFFAOYSA-N 0.000 description 1
- 238000010533 azeotropic distillation Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000001721 carbon Chemical class 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 230000003013 cytotoxicity Effects 0.000 description 1
- 231100000135 cytotoxicity Toxicity 0.000 description 1
- DFHIFRBDQIFRFB-UHFFFAOYSA-N decane-1,10-diamine;dihydrochloride Chemical compound [Cl-].[Cl-].[NH3+]CCCCCCCCCC[NH3+] DFHIFRBDQIFRFB-UHFFFAOYSA-N 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- 229940043279 diisopropylamine Drugs 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 1
- CEIPQQODRKXDSB-UHFFFAOYSA-N ethyl 3-(6-hydroxynaphthalen-2-yl)-1H-indazole-5-carboximidate dihydrochloride Chemical compound Cl.Cl.C1=C(O)C=CC2=CC(C3=NNC4=CC=C(C=C43)C(=N)OCC)=CC=C21 CEIPQQODRKXDSB-UHFFFAOYSA-N 0.000 description 1
- XGGHCMUJAUKPIJ-UHFFFAOYSA-N ethyl n-prop-2-ynylcarbamate Chemical compound CCOC(=O)NCC#C XGGHCMUJAUKPIJ-UHFFFAOYSA-N 0.000 description 1
- RHXUZKJNHAMZEP-LWTKGLMZSA-N europium;(z)-5-hydroxy-2,2,6,6-tetramethylhept-4-en-3-one Chemical compound [Eu].CC(C)(C)C(\O)=C\C(=O)C(C)(C)C.CC(C)(C)C(\O)=C\C(=O)C(C)(C)C.CC(C)(C)C(\O)=C\C(=O)C(C)(C)C RHXUZKJNHAMZEP-LWTKGLMZSA-N 0.000 description 1
- FIMAYKDZLLQUDW-UHFFFAOYSA-N fluoro(dioxido)borane;trimethyloxidanium Chemical compound C[O+](C)C.C[O+](C)C.[O-]B([O-])F FIMAYKDZLLQUDW-UHFFFAOYSA-N 0.000 description 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
- BTCSSZJGUNDROE-UHFFFAOYSA-N gamma-aminobutyric acid Chemical compound NCCCC(O)=O BTCSSZJGUNDROE-UHFFFAOYSA-N 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 239000012433 hydrogen halide Substances 0.000 description 1
- 229910000039 hydrogen halide Inorganic materials 0.000 description 1
- 238000007327 hydrogenolysis reaction Methods 0.000 description 1
- 150000001261 hydroxy acids Chemical class 0.000 description 1
- 238000007031 hydroxymethylation reaction Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
- DXASQZJWWGZNSF-UHFFFAOYSA-N n,n-dimethylmethanamine;sulfur trioxide Chemical group CN(C)C.O=S(=O)=O DXASQZJWWGZNSF-UHFFFAOYSA-N 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 229910000069 nitrogen hydride Inorganic materials 0.000 description 1
- 239000012038 nucleophile Substances 0.000 description 1
- 238000010534 nucleophilic substitution reaction Methods 0.000 description 1
- 239000010502 orange oil Substances 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000012746 preparative thin layer chromatography Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 239000003579 shift reagent Substances 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- BAZAXWOYCMUHIX-UHFFFAOYSA-M sodium perchlorate Chemical compound [Na+].[O-]Cl(=O)(=O)=O BAZAXWOYCMUHIX-UHFFFAOYSA-M 0.000 description 1
- 229910001488 sodium perchlorate Inorganic materials 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- VSWLXYAZJZQIKA-UHFFFAOYSA-N tetrachloromethane;triphenylphosphane Chemical compound ClC(Cl)(Cl)Cl.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 VSWLXYAZJZQIKA-UHFFFAOYSA-N 0.000 description 1
- DGQOCLATAPFASR-UHFFFAOYSA-N tetrahydroxy-1,4-benzoquinone Chemical compound OC1=C(O)C(=O)C(O)=C(O)C1=O DGQOCLATAPFASR-UHFFFAOYSA-N 0.000 description 1
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
- 229940124597 therapeutic agent Drugs 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
- C07D471/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
Definitions
- the present invention relates to chemical processes and novel chemical intermediates which are useful for preparing pharmaceutically important camptothecin analogues such as (S)- 10-[(dimethylamino)methyl]-4-ethyl-4,9-dihydroxy-lH-pyrano[3',4':6,7]indolizino[l,2- b]quinoline-3,14(4H,12 )dione monohydrochloride, commonly known as topotecan; or (S)- 4-ethyl-4,9-dihydroxy- lH-pyrano[3'4':6,7 ⁇ indolizino[ 1 ,2-b]quinoline-3, 14(4H, 12H)dione, commonly known as 10-methoxycamptothecin, in high enantiomeiic excess.
- camptothecin analogues such as (S)- 10-[(dimethylamino)methyl]-4-ethyl-4,9-dihydroxy-lH-pyrano
- Camptothecin analogues such as topotecan have been shown to be useful as both antineoplastic and antiviral therapeutic agents.
- a recent example of a different total synthesis was published by Comins, et al., J. Am. Chem. Soc, 114, 10971, 1992.
- optimal therapeutic activity is provided by only one configuration of the molecule. It is therefore desirable to produce this material in a form which is highly enriched in only one absolute configuration of the chiral center.
- An object of this invention is to provide novel chemical intermediates which are useful in the asymmetric synthesis of camptothecin analogues.
- Another object of the present invention is to provide processes for preparing chemical intermediates useful in the asymmetric synthesis of camptothecin analogues.
- this invention provides compounds according to Formulae (I), (II) or
- X is selected from a group consisting essentially of a cyano group; a carboxylic acid; an N-aryl carboxylic acid derivative of Formula (A);
- (A) and a good leaving group preferably a halide not including chloride, yet more preferably a bromide or iodide, most preferably bromide; or a sulfonate, more preferably a/?-fluorobenzenesulfonate, trifluoromethanesulfonate or fluorosulphonate, most preferably trifluoromethanesulfonate;
- Y is selected from a group consisting essentially of a cyano group; a carboxylic acid; an N-aryl carboxylic acid derivative of Formula (A);
- (A) and a good leaving group preferably a halide, more preferably a chloride, bromide or iodide, most preferably bromide; or a sulfonate, more preferably a p-fluorobenzenesulfonate, trifluoromethanesulfonate or fluorosulphonate, most preferably trifluoromethanesulfonate;
- R is propargyl (i.e., -CH2C ⁇ CH) or substituted propargyl, as in Formula (B);
- R is hydrogen, or Rj together with R2 is -OCH2O-;
- R2 is hydrogen; O(Ci-C6) alkyl, preferably methoxy; OH; or Rj together with R2 is -OCH 2 O-;
- R3 is hydrogen; OH; O(Ci-C6) alkyl; NO2; NH2; or a protected nitrogen group which can be converted to NH2, preferably trifluoroacetamido, acetamido, methoxycarbonylamino or carboxenzyloxyamino;
- R4 is hydrogen; SiMe3; or alkyl, preferably methyl or ethyl;
- R5 is hydrogen or COOR6
- R6 is a carboxylic acid ester group, preferably methyl, ethyl, /z-propyl, isopropyl, n-butyl, j-butyl, t-butyl, allyl or benzyl esters; and
- R7 and R8 are both hydrogen or R7 together with R8 is CH(t-butyl).
- this invention provides novel methods for the asymmetric total synthesis of camptothecin analogues.
- camptothecin analogues primarily result in racemic products.
- the antiviral or antineoplastic activity of camptothecin analogues has been observed to vary with enantiomeric purity. That is, one enantiomer of a given analogue exhibits superior antiviral or antineoplastic activity when compared with that of the other enantiomer.
- the unnatural enantiomer of camptothecin (R) exhibits cytotoxicity without having the specific anticancer activity associated with the naturally-occurring enantiomer (S).
- the compounds of the present invention represented by the Formulae (I), (II), and (in):
- X is selected from a group consisting essentially of a cyano group; a carboxylic acid; an N-aryl carboxylic acid derivative of Formula (A);
- (A) and a good leaving group preferably a halide not including chloride, more preferably a bromide or iodide, most preferably bromide; or a sulfonate, more preferably ap-fluorobenzenesulfonate, trifluoromethanesulfonate or fluorosulphonate, most preferably trifluoromethanesulfonate;
- Y is selected from a group consisting essentially of a cyano group; a carboxylic acid; an N-aryl carboxylic acid derivative of Formula (A);
- (A) and a good leaving group preferably a halide, more preferably a chloride, bromide or iodide, most preferably bromide; or a sulfonate, more preferably a p-fluorobenzenesulfonate, trifluoromethanesulfonate or fluorosulphonate, most preferably trifluoromethanesulfonate;
- R is propargyl (i.e., -CH2C ⁇ CH) or substituted propargyl, as in Formula (B);
- R ⁇ is hydrogen, or R ⁇ together with R2 is -OCH2O-;
- R2 is hydrogen; O(Ci-C6) alkyl, preferably methoxy; OH; or Rj together with R2 is -OCH 2 O;
- R3 is hydrogen; OH; O(C ⁇ -C6) alkyl; NO2; H2; or a protected nitrogen group which can be converted to NH2, preferably, trifluoroacetamido, acetamido, methoxycarbonylamino or carboxenzyloxyamino;
- R4 is hydrogen; SiMe3; or alkyl, preferably, methyl or ethyl;
- R5 is hydrogen or COOR6;
- R6 is a carboxylic acid ester group, preferably methyl, ethyl, /i-propyl, isopropyl, n-butyl, 5-butyl, t-butyl, allyl or benzyl esters; and
- R7 and R ⁇ are both hydrogen or R7 together with R8 is CH(t-butyl),
- camptothecin analogues are useful as chemical intermediates in the production of camptothecin analogues by the asymmetric syntheses of the present invention.
- good leaving group means any chemical moiety which one of ordinary skill in the art would understand to be sufficiently electrophilic so as to readily undergo nucleophilic substitution in the presence of a nucleophile, for example chloride, bromide, iodide, p- fluorobenzenesulfonate, trifluoromethylsulfonate or fluorosulphonate.
- protected nitrogen group which can be converted to NH2 includes any chemical moiety which one of ordinary skill in the art would understand to be the protected equivalent of -NH2 and capable of readily being deprotected by known methods to -NH2, preferably trifluoroacetamido, acetamido, methoxycarbonylamino or carboxenzyloxyamino.
- alkyl includes common C1-C6 saturated hydrocarbon chains such as methyl, ethyl, n-propyl, isopropyl, n-butyl, s-butyl and t-butyl.
- camptothecin includes camptothecin and any derivative thereof the structure of which is based on the lH-pyrano[3',4':6,7]indolizino-[l,2-b]quinolin-3,14(4H,12H)-dione ring system.
- carboxylic acid refers to -COOH.
- cyano group refers to C ⁇ N.
- carboxylic acid ester groups refers to methyl, ethyl, n-propyl, isopropyl, n- butyl, _y-butyl, t-butyl, allyl and benzyl esters.
- strong alkylating agent includes agents capable of producing either an O- alkylimidate or imidate ester, imidoyl halide, or imide derivative in the process of the present invention.
- the first process of the present invention is illustrated in Schemes 1-4.
- this process comprises: a) forming a chiral cis dioxolanone having a carboxylic acid function, the cis dioxolanone having the absolute configuration desired in the camptothecin analogue; b) forming a pyrrolo[3,4-b]quinoline having a free amine function; c) reacting the cis dioxolanone with the pyrrolo[3,4-b]quinoline to form a compound of Formula (III)
- R j is hydrogen or R ⁇ together with R2 is -OCH2O-, preferably hydrogen;
- R2 is hydrogen; O(C ⁇ -C6)alkyl, preferably methoxy; OH; or R together with R2 is -OCH 2 O-;
- R3 is hydrogen; OH; O(C ⁇ -C(5)alkyl; NO2; NH2; or a protected nitrogen which can be converted to NH2, preferably hydrogen;
- R4 is hydrogen; SiMe3; or alkyl, preferably hydrogen or alkyl, the most preferred alkyl being ethyl;
- R5 is hydrogen or COORg
- R6 is a carboxylic acid ester group, preferably methyl, ethyl, n-propyl, isopropyl, n- butyl, 5-butyl, t-butyl, allyl or benzyl esters, most preferably methyl ester, and R7 and R together form CH(t-butyl); and d) converting the compound of Formula (III) into a camptothecin analogue.
- Schemes 6 and 7 illustrate the second process of the present invention.
- this process comprises: a) forming a chiral cis dioxolanone having the absolute configuration desired in the camptothecin analogue; b) converting the cis dioxolanone to a compound of Formula (I)
- X is selected from a group consisting of a good leaving group, preferably a halide not including chloride, more preferably a bromide or iodide; or a sulfonate, more preferably, p-fluorobenzenesulfonate, trifluoromethanesulfonate or fluorosulphonate; a cyano group; a carboxylic acid; and an N-aryl carboxylic amide derivative of Formula (A);
- R is propargyl or substituted propargyl of Formula (B);
- Y is selected from a group consisting of a good leaving group, a cyano group, a carboxylic acid, and an N-aryl carboxylic amide derivative of Formula (A);
- Chiral l,3-dioxalan-4-one is prepared from commercially available R-2-aminobutyric acid. Diazotisation of the amino acid with sodium nitrite and sulfuric acid is accompanied by the displacement of the diazo group with complete retention of configuration to give R-2- hydroxybutyric acid. Similar reactions have been described by K. Mori, et al. in Tetrahedron, 35, 1601, 1979. The chiral hydroxyl-bearing carbon eventually becomes the chiral center (C- 20) of the camptothecin molecule. This hydroxyacid is converted to the corresponding acetal, (1) in Scheme 1, with a very high stereoselectivity (greater than 20: 1) for formation of the cis dioxolanone.
- Step a) of the first process is described as follows.
- Scheme 1 illustrates a process for making the dioxolanone starting material.
- Scheme 2 Knoevenagel condensation of the commercially available mono-methyl acetal of glyoxaldehyde with methylbenzylmalonate gives methylene malonate (2).
- enolate preferably the lithium enolate
- compound (3) in which the stereochemistry of the dioxolanone is as shown.
- step b) of the first process of the present invention the substituted pyrrolo[3,4- blquinoline (6) is prepared as shown in Scheme 3.
- R ⁇ r ⁇ -anisidine is acylated on nitrogen using bromoacetyl bromide (or optionally, chloroacetyl chloride).
- the remaining, alkyl bromide (or chloride) group is subsequently displaced in an SN2 reaction using propargylamine, and the secondary amine nitrogen is protected by forming the corresponding carbamate derivative with methyl chloroformate to yield (5).
- Compound (5) is reacted in a polar solvent, preferably methylene chloride, 1 ,2-dichloroethane, 1,2-dimethoxyethane, tetrahydrofuran, N,N-dimethylformamide, acetonitrile, acetone or N-methylpyrrolidinone, most preferably acetonitrile; at a starting temperature of about -30°C, followed by warming to a temperature of about 20-85°C, preferably at 40-85°C, most preferably at a temperature of 40- 50°C; in the presence of a strong alkylating agent or such agent as is capable of producing either an O-alkylimidate or imidate ester, imidoyl halide, or such imide derivative defined herein and throughout this application as "imidate/imidoyl halide derivative”; preferably trifluoromethanesulfonic anhydride, dimethylsulfate, alkyloxonium tetrafluoroborates,
- the resulting imidate ⁇ midoyl halide derivative then undergoes [4+2] cycloaddition and subsequent elimination of methanol (in the case in which an O-methyl imidate ester is initially formed) or hydrogen halide (in the case in which an imidoyl halide is initially formed) or a sulfonic acid (in the case in which an imidate ester is initially formed) to yield a substituted pyrrolo[3,4-b]quinoline (6).
- This transformation has also been described in U.S. Serial No. 07/941,496.
- step c) of the first process of the present invention the carboxylic acid functionality of the cis dioxolanone is reacted with the pyrrolo[3,4-b]quinoline at the amine function to form an amide having a dimethyl acetal function.
- This dimethyl acetal function of the amide is then hydrolyzed to form an aldehyde. Intramolecular aldol condensation of this aldehyde, followed by aromatization, yields a compound of Formula (III).
- amine (7) is prepared from (6) by hydrolysis of the carbamate function with acetic acid saturated with hydrobromic acid as shown in Scheme 4.
- This intermediate is coupled with the carboxylic acid (4) prepared as in Scheme 2 by utilizing l-(3- dimethylaminopropyl)-3-ethylcarbodiimide (abbreviated WSCD for "water-soluble carbodiimide” in the Scheme) and hydroxybenzotriazole (abbreviated HOBT) to give the resulting amide (8).
- WSCD l-(3- dimethylaminopropyl)-3-ethylcarbodiimide
- HOBT hydroxybenzotriazole
- the dimethyl acetal function is hydrolyzed with boron trifluoride etherate to give the resulting aldehyde (9).
- step d) of the first process of the present invention this intermediate of Formula (El), wherein R5 is methyl ester, undergoes reduction at the methyl ester to an alcohol function, followed by intramolecular lactone formation to form a camptothecin analogue.
- this intermediate of Formula (El) undergoes reduction at the methyl ester to an alcohol function, followed by intramolecular lactone formation to form a camptothecin analogue.
- subsequent reduction of the methyl ester of (10a) to the corresponding alcohol and closure of the E ring lactone by basic hydrolysis of the dioxolanone ring and subsequent acidification gives an asymmetric total synthesis of (S)-lO-methoxycamptothecin (11).
- step c) of the first process reacting a cis dioxolanone with a pyrrolo[3,4-b]quinoline also results in a product of Formula (HI), wherein R5 is hydrogen.
- this compound is converted to a camptothecin analogue by a process comprising:
- compound (10b) By utilizing a reactive, pre-formed Mannich reagent (1,1,3,3-tetramethyl-diaminomethane), compound (10b) can be very readily N,N-dimethylaminomethylated (rather than hydroxymethylated).
- This intermediate is not isolated (refer to Scheme 4) but rather worked up by sequential treatment with aqueous base to displace dimethylamine and concurrently hydrolyze the acetal of the dioxolanone ring. This is followed by acidification to close the lactone ring and precipitate the desired product, (S)-10- methoxycamptothecin in very good (65%) overall yield.
- a second process of the present invention for the synthesis of camptothecins possessing the natural enantiomeric configuration can also be executed utilizing chiral dioxolanone (1).
- This process which is outlined in Schemes 6 and 7, is substantially different from the above-described process of the present invention.
- the chiral cis dioxolanone having a diester function described in step a) of the second process can be formed by Michael addition of an enolate of dioxolanone to diethyl glutaconate.
- the dioxolanone enolate derived from (1) is added in a Michael fashion (1,4-addition) to diethyl glutaconate to give diester (12).
- step b) of the second process the cis dioxolanone is converted to a compound of Formula (I), wherein X is preferably a good leaving group, more preferably chloride, bromide or iodide, most preferably bromide, by hydrolysis of the diester function of the dioxolanone, followed by ring closure to form a corresponding glutarimide and treatment of the glutarimide with an excess of a thionyl halide, preferably thionyl bromide, in dimethylformamide, followed by workup in aqueous base. The diester is then in this fashion hydrolyzed and ring-closed to give the corresponding glutarimide (13) by treatment with ammonia in acetic acid.
- X is preferably a good leaving group, more preferably chloride, bromide or iodide, most preferably bromide
- the glutarimide is then treated with excess thionyl chloride or thionyl bromide in the presence of N,N-dimethylformamide. Workup with aqueous base, followed by neutralization results in the formation of bicyclic intermediate (14a). While not wishing to be bound to any particular mechanism of action, it is believed that this step proceeds by the following mechanism.
- Thionyl halide converts N,N-dimethylformamide into the corresponding N,N-dimethyliminium halide (Vilsmeier reagent) which serves to formylate the glutarimide ring at a position adjacent to one of the carbonyl groups.
- a compound of Formula (I) wherein X is a sulfonate, preferably, p-fluorobenzenesulfonate, trifluoromethanesulfonate and fluorosulphonate, most preferably trifluoromethanesulfonate (compound (13)) may be treated with a powerful sulfonylating agent such as trifluoromethanesulfonic anhydride (triflic anhydride) in the presence of N,N-dimethylformamide, resulting in a product (14b) which is a vinyl sulfonate analogue of vinyl halides (14a).
- a powerful sulfonylating agent such as trifluoromethanesulfonic anhydride (triflic anhydride) in the presence of N,N-dimethylformamide, resulting in a product (14b) which is a vinyl sulfonate analogue of vinyl halides (14a).
- a second process of the present invention for the synthesis of camptothecins possessing the natural enantiomeric configuration can also be executed utilizing chiral dioxolanone (1).
- This process which is outlined in Schemes 6 and 7, is substantially different from the above-described process of the present invention.
- the chiral cis dioxolanone having a diester function described in step a) of the second process can be formed by Michael addition of an enolate of dioxolanone to diethyl glutaconate.
- the dioxolanone enolate derived from (1) is added in a Michael fashion (1,4-addition) to diethyl glutaconate to give diester (12).
- step b) of the second process the cis dioxolanone is converted to a compound of Formula (I), wherein X is preferably a good leaving group, more preferably chloride, bromide or iodide, most preferably bromide, by hydrolysis of the diester function of the dioxolanone, followed by ring closure to fo ⁇ n a corresponding glutarimide and treatment of the glutarimide with an excess of a thionyl halide, preferably thionyl bromide, in dimethylformamide, followed by workup in aqueous base.
- X is preferably a good leaving group, more preferably chloride, bromide or iodide, most preferably bromide
- the diester is then in this fashion hydrolyzed and ring-closed to give the corresponding glutarimide (13) by treatment with ammonia in acetic acid.
- the glutarimide is then treated with excess thionyl chloride or thionyl bromide in the presence of N,N-dimethylformamide. Workup with aqueous base, followed by neutralization results in the formation of bicyclic intermediate (14a). While not wishing to be bound to any particular mechanism of action, it is believed that this step proceeds by the following mechanism.
- Thionyl halide converts N,N-dimethylformamide into the corresponding N,N-dimethyliminium halide (Vilsmeier reagent) which serves to formylate the glutarimide ring at a position adjacent to one of the carbonyl groups.
- the other carbonyl group of the glutarimide is converted in the same process to the corresponding vinyl halide by the action of excess thionyl halide.
- Workup with a basic aqueous solution then generates the isolated product. During the course of workup a prototropic shift occurs, causing rearrangement of the exocyclic aldehyde function to give the corresponding hydroxymethyl pyridone.
- the hydroxymethyl group closes onto the carbonyl group of the chiral dioxolanone, ultimately resulting in loss of pivalaldehyde and formation of what will become the E ring lactone of camptothecin with an absolute configuration identical to that possessed by the natural product.
- a compound of Formula (I) wherein X is a sulfonate, preferably, p-fluorobenzenesulfonate, trifluoromethanesulfonate and fluorosulphonate, most preferably trifluoromethanesulfonate (compound (13)) may be treated with a powerful sulfonylating agent such as trifluoromethanesulfonic anhydride (triflic anhydride) in the presence of N,N-dimethylformamide, resulting in a product (14b) which is a vinyl sulfonate analogue of vinyl halides (14a).
- a powerful sulfonylating agent such as trifluoromethanesulfonic anhydride (triflic anhydride) in the presence of N,N-dimethylformamide, resulting in a product (14b) which is a vinyl sulfonate analogue of vinyl halides (14a).
- (R)-2-Hydroxybutyric acid is prepared from (R)-2-aminobutyric acid following the procedure of K. Mori et al. described in Tetrahedron, 35, 1601, 1979. The reaction product was obtained in approximately 65% yield when carried out on a scale utilizing 50 g of the starting aminobutyric acid.
- the (R)-2-aminobutyric acid was purchased from the Aldrich Chemical Corp. with a purity of 99%. The chiral purity of the desired (R)-2-hydroxybutyric acid was previously established by Mori as >97%.
- This material was distilled at a pressure of 50 mm Hg to give a main fraction (9.77 g, 82.0% yield) with boiling point of 93-95°C.
- the product was examined by 1H NMR spectroscopy and determined to be an approximately 28:1 mixture of cis- and tr ⁇ rw-dioxolanone ring isomers by comparison of the relative integrations of the methine singlets representing the -CH(tert-butyl) proton for the respective isomers.
- the product was collected by rapid decanting of the cold solution, washing with about 25 ml of -78°C hexane, and filtration at -78°C using a chilled, jacketed Buchner funnel. The collected product was quickly removed for storage and was observed to melt at approximately -5°C. The presence of the minor, trans isomer of the dioxolanone ring was no longer detectable using *H NMR spectroscopy.
- the chirality of the product was determined by 1H NMR spectroscopy using a chiral shift reagent Eu(thd)3, (tris(2,2,6,6-tetramethyl-3,5-heptanedionato)europium).
- a sample of racemic material was prepared from racemic 2-hydroxybutyric acid and recrystallized at low temperature as described above for the chiral product in order to prepare a sample for comparison.
- the dioxolanone (1) prepared as described in Step 1 (765 mg, 4.4 mmol) was dissolved in 5 ml of freshly distilled tetrahydrofuran and cooled to -78°C in a separate reaction vessel under an atmosphere of dry nitrogen. This solution was then carefully transferred to the freshly prepared solution of lithium diisopropylamide via a double-ended needle over about 10 minutes. The temperature of the lithium diisopropylamide solution was not allowed to rise above about -75°C during the course of the addition. The reaction solution was stirred for 45 minutes after the addition was complete. During this time a solution of compound (2) was prepared in 5 ml of dry tetrahydrofuran and cooled to - 78°C, again under an atmosphere of dry nitrogen.
- the solution of (2) was added dropwise over about 10 minutes to the stirred enolate solution of (1). After stirring for approximately 3 hours with gradual warming to -20°C the mixture was quenched by pouring into 30 ml of a half-saturated solution of aqueous ammonium chloride and extracted with 2 x 50 ml portions of diethyl ether. The combined organic layers were dried over anhydrous sodium sulfate, filtered and evaporated to give 1.70 g of a clear, colorless oil. The product was chromatographed on 50 g of silica gel using 20% ethyl acetate:hexane as eluent. After evaporation of solvent from the product-containing fractions, a total of 1.08 g (58.1%) of desired product was obtained as a heavy, colorless oil.
- the mixture was diluted with water (200 ml) and subsequently washed with an additional 200 ml of water and 200 ml of 3% aqueous, hydrochloric acid solution.
- the methylene chloride layer was dried over anhydrous sodium sulfate, evaporated to a yellow-green solid, and triturated with 150 ml of tert-butyl methyl ether to give a white, crystalline powder after filtration. After drying under reduced pressure, 22.5 g (92.3%) of the desired product was obtained.
- the product was chromatographed by filtration through 70 g of silica gel using 5% methanol:methylene chloride as eluent. After evaporation of solvent from the product-containing fractions the desired compound was isolated by evaporation of solvent to yield 10.0 g of a pale-orange, crystalline solid (91.7%).
- Step 8 CICOOMe, CH 2 CI 2 , pyridine. RT 0
- the residual oil was partitioned between 25 ml each of methylene chloride and water, and the aqueous phase was extracted with 3 additional 25 ml portions of methylene chloride.
- the combined organic extracts were washed with 50 ml of water, dried over anhydrous sodium sulfate, and evaporated to a brown solid.
- the solid was recrystallized from methanol to give 155 mg of product (60% yield) which was collected in two crops.
- the progress of the reaction was monitored by HPLC using a Cl8 ⁇ Bondapak column (50% acetonitrile:water containing 0.1 M sodium perchlorate adjusted to a pH of 2.5 by addition of perchloric acid; detection by UV at a wavelength of 218 nm, flow rate 2.0 ml/min; r.t. of starting amine 1.33 min., r.t. of product 9.88 min.). After 24 hours the starting material had been essentially consumed and the relative peak-area-ratio response for the major product was 93.5%. The reaction was worked up by evaporating the solvent under reduced pressure to a brown oil. The residual material was partitioned between 50 ml each of methylene chloride and water.
- a 500 mg sample of the starting acetal (0.89 mmol) was stirred in a solution of 50 ml of methylene chloride at -78°C. This was treated with 0.8 ml (923 mg, 6.5 mmol, 7.3 eq) of boron trifluoride etherate added in a single portion. The solution was stirred for 20 minutes with continued cooling, then stirred with the cooling bath removed for an additional 20 minutes. The solution was diluted with 25 ml of water, then stirred vigorously for an additional 30 minutes. The pH of the solution was then adjusted to approximately 6.0 by the addition of solid sodium bicarbonate. Stirring was stopped, and the layers of the reaction were separated.
- the crude aldehyde was dissolved in 35 ml of toluene containing two drops (about 40 mg) of trifluoroacetic acid. The mixture was refluxed for 18 hours, washed with 25 ml of a saturated solution of aqueous sodium bicarbonate and evaporated to give 500 mg of a dark oil. About 460 mg of this crude product was then carried on by dissolution in 45 ml of toluene. The toluene solution was stirred under an atmosphere of nitrogen at ambient temperature, and 460 mg (1.98 mmol, 2.2 theoretical mol eq) of 2,3-dichloro-5,6-dicyanobenzoquinone (DDQ) was added.
- DDQ 2,3-dichloro-5,6-dicyanobenzoquinone
- UV Detector UV at a wavelength of 370 nm
- Sample is first dissolved in a minimum of N,N-dimethylformamide, followed by diluting to an approximate concentration of 0.1 mg/ml in the mobile phase.
- the aqueous solution was carefully acidified to a pH of approximately 3.5 - 4.0 by the dropwise addition of 5% aqueous, hydrochloric acid solution. A solid was seen to precipitate from the aqueous solution.
- the aqueous suspension was diluted to a volume of 15 ml and extracted with 3 x 35 ml portions of 20% methanokmethylene chloride. The organic layers were then combined and evaporated to dryness under reduced pressure. The residual solid was triturated with 5 ml of hot methanol and the product was isolated by filtration. The identity of the product (9.0 mg, 65% yield) was confirmed in the same manner as for the immediately preceding reaction.
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US75063 | 1993-06-10 | ||
US08/075,063 US5405963A (en) | 1993-06-10 | 1993-06-10 | Process for asymmetric total synthesis of camptothecin analogues |
PCT/US1994/006451 WO1994029310A1 (en) | 1993-06-10 | 1994-06-09 | Process for asymmetric total synthesis of camptothecin |
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EP0705262A1 true EP0705262A1 (de) | 1996-04-10 |
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EP94919413A Withdrawn EP0705262A1 (de) | 1993-06-10 | 1994-06-09 | Verfahren zur asymmetrischen totalsynthese von camptothecin |
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US (4) | US5405963A (de) |
EP (1) | EP0705262A1 (de) |
JP (1) | JPH08511539A (de) |
AU (1) | AU7056994A (de) |
WO (1) | WO1994029310A1 (de) |
ZA (1) | ZA944090B (de) |
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US5883255A (en) * | 1990-10-31 | 1999-03-16 | Smithkline Beecham Corporation | Substituted indolizino 1,2-b!quinolinones |
US6150343A (en) * | 1993-06-30 | 2000-11-21 | University Of Pittsburgh | Camptothecin analogs and methods of preparation thereof |
US6211371B1 (en) * | 1993-06-30 | 2001-04-03 | University Of Pittsburgh | Intermediates in the synthesis of camptothecin and related compounds and synthesis thereof |
US6743917B2 (en) | 1993-06-30 | 2004-06-01 | University Of Pittsburgh | Camptothecin analogs and methods of preparation thereof |
US6136978A (en) * | 1993-06-30 | 2000-10-24 | University Of Pittsburgh | Camptothecin analogs and methods of preparation thereof |
TW438775B (en) * | 1995-04-07 | 2001-06-07 | Pharmacia & Upjohn Co Llc | Novel intermediates and process for the manufacture of camptothecin derivatives (CPT-11) and related compounds |
US5942386A (en) * | 1995-06-07 | 1999-08-24 | Thomas Jefferson University | Anti-fungal agents and methods of identifying and using the same |
WO1998007727A1 (en) * | 1996-08-19 | 1998-02-26 | Bionumerik Pharmaceuticals, Inc. | Highly lipophilic camptothecin derivatives |
US6169080B1 (en) * | 1997-02-13 | 2001-01-02 | Bionumerik Pharmaceuticals, Inc. | Highly lipophilic camptothecin derivatives |
US6207832B1 (en) | 1999-04-09 | 2001-03-27 | University Of Pittsburgh | Camptothecin analogs and methods of preparation thereof |
CA2385528C (en) | 1999-10-01 | 2013-12-10 | Immunogen, Inc. | Compositions and methods for treating cancer using immunoconjugates and chemotherapeutic agents |
EP1251115A4 (de) * | 2000-01-25 | 2008-05-14 | Kaneka Corp | Verfahren zur herstellung optisch aktiver in 2-stellung substituierter carbonsäuren |
BR0115260A (pt) * | 2000-11-09 | 2005-08-16 | Neopharm Inc | Complexos de sn-38 com lipìdeos e seus usos no tratamento de doenças |
US6372906B1 (en) | 2001-04-12 | 2002-04-16 | University Of Pittsburgh | Synthesis of silyl camptothecins and silyl homocamptothecins |
WO2003030864A1 (en) | 2001-05-29 | 2003-04-17 | Neopharm, Inc. | Liposomal formulation of irinotecan |
US6723853B2 (en) | 2001-08-27 | 2004-04-20 | University Of Pittsburgh | Intermediates and methods of preparation of intermediates in the enantiomeric synthesis of (20R)homocamptothecins and the enantiomeric synthesis of (20R)homocamptothecins |
JPWO2003068726A1 (ja) * | 2001-12-27 | 2005-06-02 | ダイセル化学工業株式会社 | 脂環式アミンのアミド誘導体とその製造法 |
CN106588837B (zh) * | 2016-10-28 | 2019-04-05 | 江西凡生实业有限公司 | 2,5-二甲基-4-羟基-3(2h)呋喃酮的制备方法 |
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US5258516A (en) * | 1990-12-20 | 1993-11-02 | Nc State University | Optically pure D,E ring intermediates useful for the synthesis of camptothecin and camptothecin analogs |
US5162532A (en) * | 1990-12-20 | 1992-11-10 | North Carolina State University | Intermediates and method of making camptothecin and camptothecin analogs |
US5247089A (en) * | 1990-12-20 | 1993-09-21 | North Carolina State University | Method of making intermediates useful for the manufacture of camptothecin and camptothecin analogs |
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1993
- 1993-06-10 US US08/075,063 patent/US5405963A/en not_active Expired - Fee Related
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1994
- 1994-06-09 EP EP94919413A patent/EP0705262A1/de not_active Withdrawn
- 1994-06-09 JP JP7502062A patent/JPH08511539A/ja active Pending
- 1994-06-09 WO PCT/US1994/006451 patent/WO1994029310A1/en not_active Application Discontinuation
- 1994-06-09 AU AU70569/94A patent/AU7056994A/en not_active Abandoned
- 1994-06-10 ZA ZA944090A patent/ZA944090B/xx unknown
- 1994-12-23 US US08/363,502 patent/US5468859A/en not_active Expired - Fee Related
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1996
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Non-Patent Citations (3)
Title |
---|
JOURNAL OF ORGANIC CHEMISTRY., vol.40, no.14, 1975, EASTON US pages 2140 - 2142 E. J. COREY 'A total synthesis of natural 20(S)-camptothecin' * |
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY., vol.114, no.27, 1992, GASTON, PA US pages 10971 - 10972 D. L. COMINS ET AL 'A 10-step, asymmetric synthesis of (S)-camptothecin' * |
See also references of WO9429310A1 * |
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US5700939A (en) | 1997-12-23 |
WO1994029310A1 (en) | 1994-12-22 |
AU7056994A (en) | 1995-01-03 |
US5468859A (en) | 1995-11-21 |
JPH08511539A (ja) | 1996-12-03 |
US5405963A (en) | 1995-04-11 |
EP0705262A4 (de) | 1996-02-13 |
ZA944090B (en) | 1995-02-21 |
US5541329A (en) | 1996-07-30 |
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